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Identifying genetic risk factors for osteoporosis.
Full Abstract
Over the past decades epidemiological research of so-called "complex" diseases, i.e., common age-related disorders such as cancer, cardiovascular disease, diabetes, and osteoporosis, has identified anthropometric, behavioural, and serum parameters as risk factors. Recently, genetic polymorphisms have gained considerable interest, propelled by the Human Genome Project and its sequela that have identified most genes and uncovered a plethora of polymorphic variants, some of which embody the genetic risk factors. In all fields of complex disease genetics (including osteoporosis) progress in identifying these genetic factors has been hampered by often controversial results. Because of the small effect size for each individual risk polymorphism, this is mostly due to low statistical power and limitations of analytical methods. Genome-wide scanning approaches can be used to find the responsible genes. It is by now clear that linkage analysis is not suitable for this, but genome-wide association analysis has much better possibilities, as is illustrated by successful identification of risk alleles for several complex diseases. Candidate gene association analysis followed by replication and prospective multi-centred meta-analysis, is currently the best way forward to identify genetic markers for complex traits, such as osteoporosis. To accomplish this, we need large (global) collaborative studies using standardized methodology and definitions, to quantify by meta-analysis the subtle effects of the responsible gene variants.
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Author information
Author/s: Uitterlinden, A G (AG); van Meurs, J B J (JB); Rivadeneira, F (F); Pols, H A P (HA);
Affiliation: Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, The Netherlands. a.g.uitterlinden(-atsign-)erasmusmc.nl
Journal and publication information
Publication Type: Journal Article; Review
Journal: Journal of musculoskeletal & neuronal interactions (J Musculoskelet Neuronal Interact), published in Greece. (Language: eng)
Reference: -2006 Jan-Mar; vol 6 (issue 1) : pp 16-26
Dates: Created 2006/05/05; Completed 2006/06/23; Revised 2007/11/15;
PMID: 16675886, status: MEDLINE (last retrieval date: 12/26/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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